Canonical Allele Identifier: CA1409673990
Gene: LINC02045 HGNC NCBI

Linked Data

dbSNP Id: rs530463411
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148217774C>T , CM000665.2:g.148217774C>T GRCh38
NC_000003.11:g.147935561C>T , CM000665.1:g.147935561C>T GRCh37
NC_000003.10:g.149418251C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924565.1:n.86+2736G>A
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